Severity 4 of 5
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Nissan is recalling 2016 Rogue vehicles because the front passenger seat frames may be improperly welded, which could increase the risk of injury in a crash.
Altec Industries is recalling 1992-2000 Aerial Cable Placer AP45 vehicles because boom tips may crack and fail, increasing injury risk.
Iowa Mold Tooling Co. is recalling Dominator I crane bodies because incorrect stabilizer arm locking pins may fail to engage, allowing the arm to extend while driving.
Pride of Iowa Sandwiches is recalling approximately 231 pounds of ready-to-eat chicken, pork, and beef products produced without federal inspection. The items were distributed to vending machines in Iowa, North Dakota, and South Dakota.
PACCAR is recalling 2017 Peterbilt 320 trucks because an undersized parking brake chamber may allow the vehicle to move unexpectedly, increasing crash risk.
Forest River is recalling 2017-2018 Dynamax Isata motorhomes because a specific water pump may leak coolant, increasing the risk of an engine compartment fire.
Forest River is recalling 2017-2018 Wolf Pack, Vengeance, and XLR trailers because the generator exhaust pipe is mounted too close to the plastic underbelly, increasing fire risk.
Empire Kosher Poultry is recalling raw chicken breast products that may contain metal. The recall was initiated after an employee observed foreign material during routine duties.
Honda is recalling 2017 Civic Sedans and Coupes because a defective halfshaft may break, potentially causing the vehicle to roll away and increasing crash risk.
Pacific Coast Fruit Company is voluntarily recalling Cauliflower Tabouleh kits due to potential Listeria monocytogenes contamination.
Cooperstown Cheese Company is recalling Roasted Garlic Cheddar cheese due to potential Listeria monocytogenes contamination. The recall covers 23 wheels distributed in New York.
Greencore USA is recalling Hannaford Egg Salad Club Rolls due to potential Listeria monocytogenes contamination. The product was distributed in seven northeastern states.
Teleflex is recalling specific Percuvance surgical instruments because the tool tip jaws may break, causing fragments to fall off during use.
Biosense Webster is recalling THERMOCOOL SF NAV catheters because a system alert may cause physicians to ablate in unintended areas.
SCA Pharmaceuticals is recalling 450 bags of oxyTOCIN 30 units in Lactated Ringers due to a lack of assurance of sterility.
Triple B Corporation is recalling Broccoli Salad Kits due to possible Listeria monocytogenes contamination from recalled broccoli supplied by Mann Packing.
Triple B Corporation is recalling Thai Veggie Kits due to possible Listeria monocytogenes contamination from recalled broccoli.
SCA Pharmaceuticals is recalling 487 syringes of Rocuronium Bromide 10 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.
Whole Foods Market is recalling Bay Cities Produce Vegetable Blend Power SB because it contains ingredients recalled for potential Listeria monocytogenes contamination.
Pacific Coast Fruit Company is voluntarily recalling bagged processed salads, including vegetable trays, due to potential Listeria monocytogenes contamination.
Triple B Corporation is recalling Super Slaw salad kits due to possible Listeria monocytogenes contamination from recalled broccoli.
Triple B Corporation is recalling Veggie Tray w/Dip products due to possible Listeria monocytogenes contamination from recalled broccoli.
SCA Pharmaceuticals is recalling 76 bags of Calcium Gluconate 2 g in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Triple B Corporation is recalling Stir Fry Kits due to possible Listeria monocytogenes contamination from broccoli supplied by Mann Packing.
Biosense Webster is recalling 19 THERMOCOOL catheters because they trigger a false magnetic distortion alert on the CARTO 3 System, potentially leading to unintended ablation.